反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
CONDITIONS
反应条件
- 温度
- 100 °C
PROCEDURE
实验过程
Enantiomer 1 of (cis)-benzyl 4-(2-([1,2,4]triazolo[4,3-a]pyridin-3-yl)quinolin-8-yloxy)-3-fluoropiperidine-1-carboxylate (0.185 g, 0.372 mmol) was dissolved in dioxane (4.6 mL) and treated with 6 M hydrogen chloride (4.65 mL, 27.9 mmol) and the reaction mixture was heated at 100° C. for 2 hours. The reaction was cooled and carefully neutralized with solid NaHCO3. The resulting aqueous layer (pH 8-9) was extracted four times with methylene chloride and the resulting organic layers were combined and dried over Na2SO4 then concentrated in vacuo. The residue was chromatographed on SiO2 eluting with a gradient of 6% NH4OH in MeOH)/methylene chloride. The desired material was isolated as a colorless film (22 mg). MS APCI (+) m/z 364.1 (M+1) detected.
WORKUP
后处理
- temperatureThe reaction was cooled
- extractionThe resulting aqueous layer (pH 8-9) was extracted four times with methylene chloride
- dry with materialdried over Na2SO4
- concentrationthen concentrated in vacuo
- customThe residue was chromatographed on SiO2 eluting with a gradient of 6% NH4OH in MeOH)/methylene chloride